Villar M T, Bass P, Dewhurst G, Theaker J M, Dathan J R
Department of Nephrology, Royal South Hants Hospital, Southampton, UK.
Nephron. 1992;62(2):226-8. doi: 10.1159/000187038.
Two patients with autosomal dominant polycystic kidney disease (ADPKD) and concurrent glomerulonephritis are described. Both developed nephrotic-range proteinuria and one showed a concomitant acceleration in the rate of decline of renal function. Subsequent open renal biopsy revealed membrano-proliferative type-1 and mesangio-proliferative glomerulonephritis, respectively. Nephrotic-range proteinuria in the presence of ADPKD, with or without an accompanying decline in renal function, should prompt further investigation to exclude coexisting glomerular disease.
本文描述了两名患有常染色体显性多囊肾病(ADPKD)并并发肾小球肾炎的患者。两名患者均出现肾病范围蛋白尿,其中一名患者肾功能下降速率同时加快。随后的开放性肾活检分别显示为1型膜增生性和系膜增生性肾小球肾炎。在ADPKD患者中出现肾病范围蛋白尿,无论是否伴有肾功能下降,均应促使进一步检查以排除并存的肾小球疾病。